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Showing 1 to 4 of 4 for “"Iodane"”.

  1. SYNTHESES AND ESTROGENICITY STUDY OF DIETHYLSTILBESTROL AND BISPHENOL-A ANALOGS AS POTENTIAL REPLACEMENT FOR BISPHENOL-A AND INVESTIGATION ON NOVEL REACTIONS INDUCED BY IODANE/QUATERNARY AMMONIUM HALIDES

    … respectively agreeing with our hypothesis. Iodane/quaternary ammonium halide in nitromethane was utilized to explore aromatic bromination, N-nitrosation-dealkylation, and benzoate ester formation from benzylamines. Koser's reagent was found to be a suitable iodane for aromatic bromination …

    siu-theses Repository record for SYNTHESES AND ESTROGENICITY STUDY OF DIETHYLSTILBESTROL AND BISPHENOL-A ANALOGS AS POTENTIAL REPLACEMENT FOR BISPHENOL-A AND INVESTIGATION ON NOVEL REACTIONS INDUCED BY IODANE/QUATERNARY AMMONIUM HALIDES (opens in a new tab)

  2. Towards the Development, Application and Understanding of Copper-Catalysed Alkene Functionalisation Processes Using Iodonium Salts

    … controlled by the electronic properties of the iodane employed, allowing enamide production to be biased with electron-poor iodonium salts and oxazines to be produced with electron-rich analogues. An overall scope of 38 compounds was collaboratively elaborated, with 20 synthesised personally. …

    cambridge Repository record for Towards the Development, Application and Understanding of Copper-Catalysed Alkene Functionalisation Processes Using Iodonium Salts (opens in a new tab)

  3. HYPERVALENT IODINE METHODS FOR CARBON–NITROGEN AND CARBON–CARBON BOND FORMATION

    … we demonstrate the synthetic applications of λ3-iodane reagents towards the formation of challenging carbon-carbon and carbon-nitrogen bonds in a complementary way to the methods already reported. Chapter 1 of this dissertation outlines the general electronic structure, geometry, synthesis and …

    temple Repository record for HYPERVALENT IODINE METHODS FOR CARBON–NITROGEN AND CARBON–CARBON BOND FORMATION (opens in a new tab)

  4. Développement de catalyseurs pour la réaction d'halolactonisation énantiosélective et valorisation de diazirines comme source d'azote électrophile

    … Dans ce chapitre, les composés haloiodanes seront étudiés plus en profondeur. Leurs synthèses et leurs réactivités seront étudiées afin de mieux comprendre ces composés. Par la suite, un cycle catalytique impliquant un acide de Bronsted chiral sera développé. Au troisième chapitre, …

    sherbrooke Repository record for Développement de catalyseurs pour la réaction d'halolactonisation énantiosélective et valorisation de diazirines comme source d'azote électrophile (opens in a new tab)